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HCID 54100298, 화합물 → (R)-4,4,4-trifluoro-2-methyl-N-[(S)-1-phenylethyl]butyramide

HRID 327812
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HRID 327812 반응식
[F:1][C:2]([F:18])([F:17])[CH2:3][CH:4]([CH3:16])[C:5]([NH:7][C@H:8]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[CH3:9])=[O:6]>O>[F:1][C:2]([F:17])([F:18])[CH2:3][C@@H:4]([CH3:16])[C:5]([NH:7][C@H:8]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[CH3:9])=[O:6]
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참가 물질

3

반응물 1

HCID 54100298HCID 54100298, 화합물

생성물 1

HCID 10967206(R)-4,4,4-trifluoro-2-methyl-N-[(S)-1-phenylethyl]butyramide수율 89%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

Impure 4,4,4-trifluoro-2-methyl-N-[(S)-1-phenylethyl]butyramide (94(R):6(S)) (5.0 g), prepared by a method similar to that described in step a) above, was dissolved in industrial methylated spirits (18.75 ml) by heating under reflux with stirring. Water (18.75 ml) was then added slowly, while continuing to heat the solution under reflux. The mixture was then heated under reflux for a further 45 minutes, and was then allowed to cool to room temperature, with continued stirring, overnight. The mixture was then filtered, and the crystalline product was washed with water (10 ml) and dried at 65° C. to give the title compound 4.45 g (89%). The product contained only 0.3% of the unwanted (S)-diastereomer.

후처리

  1. temperatureby heating
  2. temperatureunder reflux
  3. temperatureto heat the solution
  4. temperatureunder reflux
  5. temperatureThe mixture was then heated
  6. temperatureunder reflux for a further 45 minutes
  7. filtrationThe mixture was then filtered
  8. washthe crystalline product was washed with water (10 ml)
  9. customdried at 65° C.

출처 및 근거

ORD 기록
ord-c067e452242b46e68cdbcb0885d992ec
출처 데이터셋
uspto-grants-1993_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05274118

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